HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277850Generated: October 26, 2026
Tetrahydrofuran → 6-bromo-2,4-dimethyl-4-phenyl-1,4-dihydro-2H-3,1-benzoxazine
https://huagongshe.com/reaction/277850
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Amino-5-bromobenzophenone | HCID 99677 | — |
| Reactant | Ammonium Sulfate | HCID 6097028 | — |
| Product | 6-bromo-2,4-dimethyl-4-phenyl-1,4-dihydro-2H-3,1-benzoxazine | HCID 23435582 | 70% |
Reaction Steps
To a solution of (2-amino-5-bromophenyl)(phenyl)methanone (1 g, 3.6 mmol) in anhydrous THF (15 mL) was added at room temperature under nitrogen methylmagnesium bromide (3M in ether, 3 mL, 9 mmol). After 3 hours, the mixture was treated with a saturated aqueous ammonium sulfate solution (30 mL) and ethyl acetate (50 mL). The organic layer was separated, dried (MgSO4), and evaporated. The residue was then dissolved in anhydrous toluene and treated at ambient temperature under nitrogen with acetylaldehyde (2 mL). After 2 minutes, the solvent was removed and residue was purified by a column chromatography (silica gel, hexane:ethyl acetate/4:1) to afford 6-bromo-2,4-dimethyl-4-phenyl-1,4-dihydro-2H-3,1-benzoxazine as a yellowish solid (0.8 g, 70%): MS (ESI) m/z 318/320 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06358948B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-17c8211cb7114634b6ed69e28a18cb2c |
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| Source note | uspto-grants-2002_03 |
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